(M35.6) Relapsing panniculitis [weber-christian]

More details coming soon

Icon
1 701 105 in individuals diagnosis relapsing panniculitis [weber-christian] confirmed
Icon
24 040 deaths with diagnosis relapsing panniculitis [weber-christian]
Icon
1% mortality rate associated with the disease relapsing panniculitis [weber-christian]

Diagnosis relapsing panniculitis [weber-christian] is diagnosed Women are 54.83% more likely than Men

384 222

Men receive the diagnosis relapsing panniculitis [weber-christian]

7 214 (1.9 %)

Died from this diagnosis.

100
95
90
85
80
75
70
65
60
55
50
45
40
35
30
25
20
15
10
5
0
1 316 883

Women receive the diagnosis relapsing panniculitis [weber-christian]

16 826 (1.3 %)

Died from this diagnosis.

Risk Group for the Disease relapsing panniculitis [weber-christian] - Men aged 75-79 and Women aged 55-59

Icon
In Men diagnosis is most often set at age 0-95+
Icon
in in men, the disease manifests at any agein in women, the disease manifests at any age
Icon
In Women diagnosis is most often set at age 0-95+

Disease Features relapsing panniculitis [weber-christian]

Icon
Absence or low individual and public risk
Icon

Relapsing panniculitis [weber-christian] - what does this mean

Weber-christian disease, also known as relapsing panniculitis, is a rare disorder characterized by recurrent episodes of inflammation of the subcutaneous fat, which can lead to scarring and fibrosis. it is believed to be an autoimmune disorder in which the body's own immune system mistakenly attacks its own fat cells. symptoms can include fever, fatigue, joint pain, and skin lesions. treatment typically involves the use of corticosteroids, immunosuppressants, and antibiotics.

What happens during the disease - relapsing panniculitis [weber-christian]

Relapsing panniculitis (weber-christian) is an inflammatory disorder of the subcutaneous fat. it is thought to be caused by an autoimmune process, in which the body's immune system mistakenly attacks the fat cells, leading to inflammation and subsequent fat necrosis. this process is characterized by recurrent episodes of inflammation followed by periods of remission. the exact cause of the autoimmune process is unknown, but is thought to be a combination of genetic and environmental factors.

Clinical Pattern

More details coming soon

How does a doctor diagnose

  • Physical examination
  • Blood tests to check for inflammation markers
  • Imaging tests such as X-rays or CT scans
  • Biopsy of the affected area
  • Skin biopsy to check for changes in the fat cells
  • Ultrasound scan to check for changes in the fat cells
Additional measures:
  • Treatment with corticosteroids
  • Immunosuppressive drugs
  • Surgery to remove the affected tissue

Treatment and Medical Assistance

Main goal: To reduce inflammation and decrease the number of relapses
  • Prescribe corticosteroids to reduce inflammation
  • Prescribe antibiotics to treat any secondary infections
  • Encourage rest and relaxation
  • Prescribe nonsteroidal anti-inflammatory drugs (NSAIDs) to reduce inflammation and pain
  • Prescribe antimalarial drugs to reduce inflammation
  • Prescribe immunosuppressants to reduce the body's immune response
  • Encourage regular exercise to improve overall health
  • Prescribe colchicine to reduce inflammation
  • Prescribe retinoids to reduce inflammation and help skin heal
  • Prescribe vitamin A supplements to help skin heal
  • Prescribe biologic medications to reduce inflammation and improve skin healing
Icon
17 Days of Hospitalization Required
Icon
Average Time for Outpatient Care Not Established

Relapsing panniculitis [weber-christian] - Prevention

Relapsing panniculitis [weber-christian] can be prevented by avoiding exposure to cold temperatures, avoiding stress, eating a healthy diet, and exercising regularly. additionally, patients should take steps to avoid infections, such as washing their hands regularly and avoiding contact with people who are ill.